首页> 美国卫生研究院文献>Frontiers in Neural Circuits >Cre-Recombinase Dependent Germline Deletion of a Conditional Allele in the Rgs9cre Mouse Line
【2h】

Cre-Recombinase Dependent Germline Deletion of a Conditional Allele in the Rgs9cre Mouse Line

机译:Rgs9cre小鼠品系中条件等位基因的Cre重组酶依赖的种系删除

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Cre-LoxP conditional knockout animals have become a prominent tool to understand gene function in discrete cell-types and neural circuits. However, this technology has significant limitations including off target cre-dependent recombination. The Rgs9cre strain has been used to generate a conditional knockout in striatal medium spiny neurons, but, as presented in the current study, off target recombination in the germline results in nonconditional deletion of LoxP alleles. Using a Rem2 conditional allele, germline deletion (GD) was observed in a sex dependent manner. When Cre and LoxP alleles were co-inherited from the female parent, 27 of 29 LoxP alleles were recombined, but when co-inherited from the male parent, 5 of 36 LoxP alleles were recombined. Rem2 expression measured by RT-qPCR confirmed nonconditional recombination in extrastriatal nuclei. Cre-LoxP is a powerful technique to modify genomic DNA (gDNA), however careful characterization of these mice is required to confirm control of conditional recombination.
机译:Cre-LoxP条件敲除动物已经成为了解离散细胞类型和神经回路中基因功能的重要工具。但是,该技术具有明显的局限性,包括脱靶的cre依赖重组。 Rgs9cre菌株已被用于在纹状体中棘神经元中产生条件性敲除,但是,如本研究所述,种系中靶标外重组导致LoxP等位基因的无条件缺失。使用Rem2条件等位基因,以性别依赖性方式观察到种系缺失(GD)。当从雌性亲本中共同继承Cre和LoxP等位基因时,将重组29个LoxP等位基因中的27个,而当从雄性亲本中共同继承时,将36个LoxP等位基因中的五个重新结合。通过RT-qPCR测量的Rem2表达证实了纹状体外核的无条件重组。 Cre-LoxP是修改基因组DNA(gDNA)的有力技术,但是需要对这些小鼠进行仔细表征以确认对条件重组的控制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号